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Q39762726-3F48B23A-C6D7-4470-8C57-44C9D87A641F
Q39762726-3F48B23A-C6D7-4470-8C57-44C9D87A641F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39762726-3F48B23A-C6D7-4470-8C57-44C9D87A641F
Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy.
P2860
Q39762726-3F48B23A-C6D7-4470-8C57-44C9D87A641F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39762726-3F48B23A-C6D7-4470-8C57-44C9D87A641F
rank
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type
BestRank
Statement
wasDerivedFrom
bd0b9c6a1eedbec38b0a852e46fcb1647fc9fb65
P2860
Whole exome sequencing in a patient with uniparental disomy of chromosome 2 and a complex phenotype.